What is Kindler syndrome? Definition, Meaning & Symptoms — Medical Dictionary
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Kindler syndrome — Definition

Kindler sendromu / Kindler syndrome
Kindler syndrome is a rare genetic skin disease. The disease is characterized by blisters, thinning and abnormal pigmentation in areas exposed to sun on the skin. It can also be seen in mucous membranes (paper, eye, genital area) precision and wound formation. This syndrome occurs as a result of mutations in FERMT1 gene and shows autozomal resesif inheritance.
Turkish
🇹🇷 Kindler sendromu
English
🇬🇧 Kindler syndrome
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Frequently Asked Questions

❓ What is Kindler sendromu?
Kindler sendromu; kindler syndrome is a rare genetic skin disease. The disease is characterized by blisters, thinning and abnormal pigmentation in areas exposed to sun on the skin. It can also be seen in mucous membranes (paper, eye, genital area) precision and wound formation. This syndrome occurs as a result of mutations in FERMT1 gene and shows autozomal resesif inheritance.
❓ What is Kindler syndrome in Turkish?
The Turkish equivalent of "Kindler syndrome" is Kindler sendromu.
❓ Which medical field is Kindler sendromu related to?
This term belongs to the Diseases category.